{"count":221277,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1646","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1644","results":[{"created":"2020-08-27T21:00:31.751109+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Fumarase deficiency for gene: FH","entity_name":"FH","entity_type":"gene"},{"created":"2020-08-27T21:00:31.455826+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Afibrinogenaemia for gene: FGG","entity_name":"FGG","entity_type":"gene"},{"created":"2020-08-27T21:00:30.938656+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Muenke syndrome for gene: FGFR3","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-08-27T21:00:30.641558+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Thanatophoric dysplasia type 1 for gene: FGFR3","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-08-27T21:00:30.339505+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Crouzon syndrome with acanthosis nigricans for gene: FGFR3","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-08-27T21:00:30.062927+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hypochondroplasia for gene: FGFR3","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-08-27T21:00:29.738421+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Achondroplasia for gene: FGFR3","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-08-27T21:00:29.439208+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Jackson-Weiss syndrome for gene: FGFR2","entity_name":"FGFR2","entity_type":"gene"},{"created":"2020-08-27T21:00:29.140055+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Beare-Stevenson cutis gyrata syndrome for gene: FGFR2","entity_name":"FGFR2","entity_type":"gene"},{"created":"2020-08-27T21:00:28.844107+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Crouzon syndrome for gene: FGFR2","entity_name":"FGFR2","entity_type":"gene"},{"created":"2020-08-27T21:00:28.331126+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Apert syndrome for gene: FGFR2","entity_name":"FGFR2","entity_type":"gene"},{"created":"2020-08-27T21:00:28.038178+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Pfeiffer syndrome for gene: FGFR2","entity_name":"FGFR2","entity_type":"gene"},{"created":"2020-08-27T21:00:27.731792+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Kallmann syndrome for gene: FGFR1","entity_name":"FGFR1","entity_type":"gene"},{"created":"2020-08-27T21:00:27.437675+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Deafness, congenital with inner ear agenesis, microtia, and microdontia for gene: FGF3","entity_name":"FGF3","entity_type":"gene"},{"created":"2020-08-27T21:00:27.142388+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Charcot-Marie-Tooth disease for gene: FGD4","entity_name":"FGD4","entity_type":"gene"},{"created":"2020-08-27T21:00:26.842394+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Aarskog-Scott syndrome for gene: FGD1","entity_name":"FGD1","entity_type":"gene"},{"created":"2020-08-27T21:00:26.542196+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Afibrinogenaemia for gene: FGB","entity_name":"FGB","entity_type":"gene"},{"created":"2020-08-27T21:00:26.246136+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Afibrinogenaemia for gene: FGA","entity_name":"FGA","entity_type":"gene"},{"created":"2020-08-27T21:00:25.736083+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Contractural arachnodactyly for gene: FBN2","entity_name":"FBN2","entity_type":"gene"},{"created":"2020-08-27T21:00:25.438554+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Marfan's syndrome for gene: FBN1","entity_name":"FBN1","entity_type":"gene"},{"created":"2020-08-27T21:00:25.138793+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cutis laxa for gene: FBLN5","entity_name":"FBLN5","entity_type":"gene"},{"created":"2020-08-27T21:00:24.842186+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Fanconi anaemia for gene: FANCI","entity_name":"FANCI","entity_type":"gene"},{"created":"2020-08-27T21:00:24.542538+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Fanconi anaemia for gene: FANCG","entity_name":"FANCG","entity_type":"gene"},{"created":"2020-08-27T21:00:24.251427+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Fanconi anaemia for gene: FANCD2","entity_name":"FANCD2","entity_type":"gene"},{"created":"2020-08-27T21:00:24.018811+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Fanconi anaemia for gene: FANCC","entity_name":"FANCC","entity_type":"gene"},{"created":"2020-08-27T21:00:23.650374+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Fanconi anaemia for gene: FANCB","entity_name":"FANCB","entity_type":"gene"},{"created":"2020-08-27T21:00:23.418656+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Fanconi anaemia for gene: FANCA","entity_name":"FANCA","entity_type":"gene"},{"created":"2020-08-27T21:00:23.124601+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Syndactyly - telecanthus - anogenital and renal malformations for gene: FAM58A","entity_name":"FAM58A","entity_type":"gene"},{"created":"2020-08-27T21:00:22.541251+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Osteosclerotic bone dysplasia for gene: FAM20C","entity_name":"FAM20C","entity_type":"gene"},{"created":"2020-08-27T21:00:22.247789+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Retinal dystrophy for gene: FAM161A","entity_name":"FAM161A","entity_type":"gene"},{"created":"2020-08-27T21:00:21.950848+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hypomyelination and congenital cataract for gene: FAM126A","entity_name":"FAM126A","entity_type":"gene"},{"created":"2020-08-27T21:00:21.718706+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Tyrosinemia, type I for gene: FAH","entity_name":"FAH","entity_type":"gene"},{"created":"2020-08-27T21:00:21.425103+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hemophilia B for gene: F9","entity_name":"F9","entity_type":"gene"},{"created":"2020-08-27T21:00:21.126180+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hemophilia A for gene: F8","entity_name":"F8","entity_type":"gene"},{"created":"2020-08-27T21:00:20.830442+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Prothrombin deficiency for gene: F2","entity_name":"F2","entity_type":"gene"},{"created":"2020-08-27T21:00:20.536153+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Factor XI deficiency for gene: F11","entity_name":"F11","entity_type":"gene"},{"created":"2020-08-27T21:00:20.235149+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Weaver syndrome 2 for gene: EZH2","entity_name":"EZH2","entity_type":"gene"},{"created":"2020-08-27T21:00:19.936867+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Deafness, autosomal dominant for gene: EYA4","entity_name":"EYA4","entity_type":"gene"},{"created":"2020-08-27T21:00:19.426015+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Branchiootorenal syndrome for gene: EYA1","entity_name":"EYA1","entity_type":"gene"},{"created":"2020-08-27T21:00:19.131280+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Exostoses, multiple, type 2 for gene: EXT2","entity_name":"EXT2","entity_type":"gene"},{"created":"2020-08-27T21:00:18.835205+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Exostoses, multiple, type 1 for gene: EXT1","entity_name":"EXT1","entity_type":"gene"},{"created":"2020-08-27T21:00:18.539099+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ellis-van Creveld syndrome for gene: EVC2","entity_name":"EVC2","entity_type":"gene"},{"created":"2020-08-27T21:00:18.244511+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ellis-van Creveld syndrome for gene: EVC","entity_name":"EVC","entity_type":"gene"},{"created":"2020-08-27T21:00:17.947044+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ethylmalonic encephalopathy for gene: ETHE1","entity_name":"ETHE1","entity_type":"gene"},{"created":"2020-08-27T21:00:17.642096+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Glutaric acidemia IIC for gene: ETFDH","entity_name":"ETFDH","entity_type":"gene"},{"created":"2020-08-27T21:00:17.349463+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Glutaric acidemia IIB for gene: ETFB","entity_name":"ETFB","entity_type":"gene"},{"created":"2020-08-27T21:00:16.837882+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Glutaric acidemia IIA for gene: ETFA","entity_name":"ETFA","entity_type":"gene"},{"created":"2020-08-27T21:00:16.541341+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hearing loss for gene: ESRRB","entity_name":"ESRRB","entity_type":"gene"},{"created":"2020-08-27T21:00:16.245486+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Roberts syndrome for gene: ESCO2","entity_name":"ESCO2","entity_type":"gene"},{"created":"2020-08-27T21:00:15.950220+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cockayne syndrome for gene: ERCC8","entity_name":"ERCC8","entity_type":"gene"},{"created":"2020-08-27T21:00:15.696804+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cockayne syndrome for gene: ERCC6","entity_name":"ERCC6","entity_type":"gene"},{"created":"2020-08-27T21:00:15.354129+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Xeroderma pigmentosum for gene: ERCC5","entity_name":"ERCC5","entity_type":"gene"},{"created":"2020-08-27T21:00:15.117456+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Xeroderma pigmentosum for gene: ERCC2","entity_name":"ERCC2","entity_type":"gene"},{"created":"2020-08-27T21:00:14.819657+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Epilepsy, progressive myoclonic 2A (Lafora) for gene: EPM2A","entity_name":"EPM2A","entity_type":"gene"},{"created":"2020-08-27T21:00:14.523398+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Arterial calcification, generalized, of infancy, 1 for gene: ENPP1","entity_name":"ENPP1","entity_type":"gene"},{"created":"2020-08-27T21:00:13.961521+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Telangiectasia, hereditary hemorrhagic, type 1 for gene: ENG","entity_name":"ENG","entity_type":"gene"},{"created":"2020-08-27T21:00:13.642483+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Muscular dystrophy, Emery-Dreifuss for gene: EMD","entity_name":"EMD","entity_type":"gene"},{"created":"2020-08-27T21:00:13.350194+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Supravalvar aortic stenosis for gene: ELN","entity_name":"ELN","entity_type":"gene"},{"created":"2020-08-27T21:00:13.062775+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Neutropenia, congenital for gene: ELANE","entity_name":"ELANE","entity_type":"gene"},{"created":"2020-08-27T21:00:12.818779+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Wolcott-Rallison syndrome for gene: EIF2AK3","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2020-08-27T21:00:12.526222+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Charcot-Marie-Tooth disease for gene: EGR2","entity_name":"EGR2","entity_type":"gene"},{"created":"2020-08-27T21:00:12.235704+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Mandibulofacial dysostosis with microcephaly for gene: EFTUD2","entity_name":"EFTUD2","entity_type":"gene"},{"created":"2020-08-27T21:00:11.935010+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Myoclonic epilepsy for gene: EFHC1","entity_name":"EFHC1","entity_type":"gene"},{"created":"2020-08-27T21:00:11.628957+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ectodermal dysplasia, hypohidrotic for gene: EDARADD","entity_name":"EDARADD","entity_type":"gene"},{"created":"2020-08-27T21:00:11.057215+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ectodermal dysplasia, hypohidrotic for gene: EDAR","entity_name":"EDAR","entity_type":"gene"},{"created":"2020-08-27T21:00:10.752216+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ectodermal dysplasia, hypohidrotic for gene: EDA","entity_name":"EDA","entity_type":"gene"},{"created":"2020-08-27T21:00:10.454725+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Miyoshi muscular dystrophy 1 for gene: DYSF","entity_name":"DYSF","entity_type":"gene"},{"created":"2020-08-27T21:00:10.218726+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Muscular dystrophy, limb-girdle, type 2B for gene: DYSF","entity_name":"DYSF","entity_type":"gene"},{"created":"2020-08-27T21:00:09.918718+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Thyroid dyshormonogenesis for gene: DUOX2","entity_name":"DUOX2","entity_type":"gene"},{"created":"2020-08-27T21:00:09.626143+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Epidermolysis bullosa, lethal acantholytic for gene: DSP","entity_name":"DSP","entity_type":"gene"},{"created":"2020-08-27T21:00:09.331014+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Congenital disorder of glycosylation, type Ij for gene: DPAGT1","entity_name":"DPAGT1","entity_type":"gene"},{"created":"2020-08-27T21:00:09.048170+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Congenital myasthenic syndrome for gene: DOK7","entity_name":"DOK7","entity_type":"gene"},{"created":"2020-08-27T21:00:08.732935+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hyper-IgE syndrome for gene: DOCK8","entity_name":"DOCK8","entity_type":"gene"},{"created":"2020-08-27T21:00:08.436017+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Immunodeficiency-centromeric instability-facial anomalies syndrome 1 for gene: DNMT3B","entity_name":"DNMT3B","entity_type":"gene"},{"created":"2020-08-27T21:00:07.850377+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Charcot-Marie-Tooth disease, axonal, type 2M for gene: DNM2","entity_name":"DNM2","entity_type":"gene"},{"created":"2020-08-27T21:00:07.549089+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Myopathy, centronuclear for gene: DNM2","entity_name":"DNM2","entity_type":"gene"},{"created":"2020-08-27T21:00:07.243870+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Muscular dystrophy, limb girdle for gene: DNAJB6","entity_name":"DNAJB6","entity_type":"gene"},{"created":"2020-08-27T21:00:06.953682+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Primary ciliary dyskinesia for gene: DNAI1","entity_name":"DNAI1","entity_type":"gene"},{"created":"2020-08-27T21:00:06.648019+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Primary ciliary dyskinesia for gene: DNAH5","entity_name":"DNAH5","entity_type":"gene"},{"created":"2020-08-27T21:00:06.406598+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Primary ciliary dyskinesia for gene: DNAH11","entity_name":"DNAH11","entity_type":"gene"},{"created":"2020-08-27T21:00:06.046527+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Primary ciliary dyskinesia for gene: DNAAF1","entity_name":"DNAAF1","entity_type":"gene"},{"created":"2020-08-27T21:00:05.743465+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Myotonic dystrophy 1 for gene: DMPK","entity_name":"DMPK","entity_type":"gene"},{"created":"2020-08-27T21:00:05.224812+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hypophosphatemic rickets, AR for gene: DMP1","entity_name":"DMP1","entity_type":"gene"},{"created":"2020-08-27T21:00:04.926756+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Becker muscular dystrophy for gene: DMD","entity_name":"DMD","entity_type":"gene"},{"created":"2020-08-27T21:00:04.626257+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Duchenne muscular dystrophy for gene: DMD","entity_name":"DMD","entity_type":"gene"},{"created":"2020-08-27T21:00:04.328442+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Spondylocostal dysostosis, autosomal recessive, 1 for gene: DLL3","entity_name":"DLL3","entity_type":"gene"},{"created":"2020-08-27T21:00:04.017461+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Maple syrup urine disease, type III for gene: DLD","entity_name":"DLD","entity_type":"gene"},{"created":"2020-08-27T21:00:03.649469+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Smith-Lemli-Opitz syndrome for gene: DHCR7","entity_name":"DHCR7","entity_type":"gene"},{"created":"2020-08-27T21:00:03.348332+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Mitochondrial DNA depletion syndrome for gene: DGUOK","entity_name":"DGUOK","entity_type":"gene"},{"created":"2020-08-27T21:00:03.053424+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hearing loss for gene: DFNB59","entity_name":"DFNB59","entity_type":"gene"},{"created":"2020-08-27T21:00:02.749657+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hearing loss for gene: DFNA5","entity_name":"DFNA5","entity_type":"gene"},{"created":"2020-08-27T21:00:02.228743+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Myopathy, myofibrillar for gene: DES","entity_name":"DES","entity_type":"gene"},{"created":"2020-08-27T21:00:01.930299+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Aromatic L-amino acid decarboxylase deficiency for gene: DDC","entity_name":"DDC","entity_type":"gene"},{"created":"2020-08-27T21:00:01.628181+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Xeroderma pigmentosum for gene: DDB2","entity_name":"DDB2","entity_type":"gene"},{"created":"2020-08-27T21:00:01.330815+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Lissencephaly, X-linked for gene: DCX","entity_name":"DCX","entity_type":"gene"},{"created":"2020-08-27T21:00:01.035195+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Severe combined immunodeficiency, Athabascan type for gene: DCLRE1C","entity_name":"DCLRE1C","entity_type":"gene"},{"created":"2020-08-27T21:00:00.736648+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Maple syrup urine disease for gene: DBT","entity_name":"DBT","entity_type":"gene"},{"created":"2020-08-27T21:00:00.433354+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes D-2-hydroxyglutaric aciduria for gene: D2HGDH","entity_name":"D2HGDH","entity_type":"gene"},{"created":"2020-08-27T21:00:00.174097+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Ichthyosis, congenital, autosomal recessive for gene: CYP4F22","entity_name":"CYP4F22","entity_type":"gene"},{"created":"2020-08-27T20:59:59.745490+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Vitamin D-dependent rickets, type I for gene: CYP27B1","entity_name":"CYP27B1","entity_type":"gene"}]}